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227305-69-3

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227305-69-3 Usage

Chemical Properties

white to light yellow crystal powde

Uses

2,3-Dihydrobenzo[b]furan-5-boronic acid is used in the suzuki-Miyaura cross-coupling reactions to prepare halogenated nucleosides.

Check Digit Verification of cas no

The CAS Registry Mumber 227305-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,3,0 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 227305-69:
(8*2)+(7*2)+(6*7)+(5*3)+(4*0)+(3*5)+(2*6)+(1*9)=123
123 % 10 = 3
So 227305-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H9BO3/c10-9(11)7-1-2-8-6(5-7)3-4-12-8/h1-2,5,10-11H,3-4H2

227305-69-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H52479)  2,3-Dihydrobenzo[b]furan-5-boronic acid, 97%   

  • 227305-69-3

  • 250mg

  • 599.0CNY

  • Detail
  • Alfa Aesar

  • (H52479)  2,3-Dihydrobenzo[b]furan-5-boronic acid, 97%   

  • 227305-69-3

  • 1g

  • 1917.0CNY

  • Detail

227305-69-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Dihydrobenzofuran-5-boronic acid

1.2 Other means of identification

Product number -
Other names 2,3-Dihydrobenzofuran-5-boronic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:227305-69-3 SDS

227305-69-3Relevant articles and documents

Multiple C-H activations to construct biologically active molecules in a process completely free of organohalogen and organometallic components

Li, Bi-Jie,Tian, Shi-Liang,Fang, Zhao,Shi, Zhang-Jie

, p. 1115 - 1118 (2008/09/21)

(Chemical Equation Presented) Step by step: Highly selective cross dehydrogenase arylation of acetanilides was developed to construct biaryls under mild condition. With this method, different aryl C-H bonds were activated in sequential reactions to construct functionalized carbazoles (see scheme), which are present as key structural units in various biological molecules and organic optical materials.

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